Jon-Ko Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Orthodontic Elastomeric Separator Module Ref K943418
Regimes: 510(k) Registry: 510(k)Orthodontic Elastomeric Chain Ref K943420
Regimes: 510(k) Registry: 510(k)Orthodontic Elastomeric Tube/Thread Ref K943417
Regimes: 510(k) Registry: 510(k)Orthodonitc Elastomeric Sleeving Ref K943421
Regimes: 510(k) Registry: 510(k)Orthodontic Elastomeric Lagature Module Ref K943419
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jon-Ko Products, Inc. have in the registry?
The registry currently lists 5 devices for Jon-Ko Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jon-Ko Products, Inc.'s devices?
Among its 5 most recently registered devices, Jon-Ko Products, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Jon-Ko Products, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Jon-Ko Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jon-Ko Products, Inc. in the registry?
The most recently registered devices listed for Jon-Ko Products, Inc. include ORTHODONTIC ELASTOMERIC SEPARATOR MODULE, ORTHODONTIC ELASTOMERIC CHAIN, ORTHODONTIC ELASTOMERIC TUBE/THREAD and ORTHODONITC ELASTOMERIC SLEEVING.